Clinical Features and Pharmacotherapy of Childhood Monoamine Neurotransmitter Disorders

por Ng, J., Heales, S. J. R., Kurian, M. A.
Publicado 2014

Hypermanganesemia due to mutations in SLC39A14: further insights into Mn deposition in the central nervous system

por Marti-Sanchez, L., Ortigoza-Escobar, J. D., Darling, A., Villaronga, M., Baide, H., Molero-Luis, M., Batllori, M., Vanegas, M. I., Muchart, J., Aquino, L., Artuch, R., Macaya, A., Kurian, M. A., Dueñas, Pérez
Publicado 2018

PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease

por Illingworth, M.A., Meyer, E., Chong, W.K., Manzur, A.Y., Carr, L.J., Younis, R., Hardy, C., McDonald, F., Childs, A.M., Stewart, B., Warren, D., Kneen, R., King, M.D., Hayflick, S.J., Kurian, M.A.
Publicado 2014